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Investigative Ophthalmology & Visual Science|August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|July 5, 2018
Comparing Clinical Perimetry and Population Receptive Field Measures in Patients with ChoroideremiaEdward H Silson, Tomas S Aleman, Aimee Willett, et al.
Molecular Vision|October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosisAlejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Human Molecular Genetics|January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathyArtur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|September 23, 2016
Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin MutationsSamuel G Jacobson, David B McGuigan, Alexander Sumaroka, et al.
Ophthalmic Genetics|March 30, 2026
Bi-allelic pathogenic variants in <i>NR2E3</i> may be associated with a subtle enhanced S-cone syndrome phenotypeAlexander Hüther, Caroline L Sherman, Alexander Sumaroka, et al.
Diabetes|March 29, 2005
Nonhuman primate models for diabetic ocular neovascularization using AAV2-mediated overexpression of vascular endothelial growth factorCorinna Lebherz, Albert M Maguire, Alberto Auricchio, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retinaArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Visual Neuroscience|January 12, 2001
Rod and cone visual cycle consequences of a null mutation in the 11-cis-retinol dehydrogenase gene in manArtur V Cideciyan, Françoise Haeseleer, Robert N Fariss, et al.
Investigative Ophthalmology & Visual Science|December 17, 2008
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutationsSamuel G Jacobson, Tomas S Aleman, Alexander Sumaroka, et al.
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